NAG-1 up-regulation mediated by EGR-1 and p53 is critical for quercetin-induced apoptosis in HCT116 colon carcinoma cells

被引:87
作者
Lim, J. H.
Park, J-W.
Min, D. S.
Chang, J-S.
Lee, Y. H.
Park, Y. B.
Choi, K. S.
Kwon, T. K.
机构
[1] Keimyung Univ, Dept Immunol, Sch Med, Taegu 700712, South Korea
[2] Daejin Univ, Dept Life Sci, Kyonggi Do, South Korea
[3] Hanyang Univ, Coll Sci & Technol, Div Mol & Life Sci, Ansan, South Korea
[4] Kyungpook Natl Univ, Coll Nat Sci, Dept Gen Engn, Taegu 702701, South Korea
[5] Ajou Univ, Sch Med, Inst Med Sci, Suwon 441749, South Korea
基金
新加坡国家研究基金会;
关键词
quercetin; NAG-1; apoptosis; Sp1; EGR-1; p53; colon carcinoma cells;
D O I
10.1007/s10495-006-0576-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Quercetin, a flavonoid molecule ubiquitously present in nature, has multiple effects on cancer cells, including the inhibition of cell proliferation and migration. However, the responsible molecular mechanisms are not fully understood. We found that quercetin induces the expression of NAG-1 (Non-steroidal anti-inflammatory drug activated gene-1), a TGF-beta superfamily protein, during quercetin-induced apoptosis of HCT116 human colon carcinoma cells. Reporter assays using the luciferase constructs containing NAG-1 promoter region demonstrate that early growth response-1 (EGR-1) and p53 are required for quercetin-mediated activation of the NAG-1 promoter. Overexpression of NAG-1 enhanced the apoptotic effect of quercetin, but suppression of quercetin-induced NAG-1 expression by NAG-1 siRNA attenuated quercetin-induced apoptosis in HCT116 cells. Taken together, the present study demonstrates for the first time that quercetin induces apoptosis via NAG-1, providing a mechanistic basis for the apoptotic effect of quercetin in colon carcinoma cells.
引用
收藏
页码:411 / 421
页数:11
相关论文
共 35 条
[1]   Anoxia induces macrophage inhibitory cytokine-1 (MIC-1) in glioblastoma cells independently of p53 and HIF-1 [J].
Albertoni, M ;
Shaw, PH ;
Nozaki, M ;
Godard, S ;
Tenan, M ;
Hamou, MF ;
Fairlie, DW ;
Breit, SN ;
Paralkar, VM ;
de Tribolet, N ;
Van Meir, EG ;
Hegi, ME .
ONCOGENE, 2002, 21 (27) :4212-4219
[2]  
Anton R, 1988, Prog Clin Biol Res, V280, P423
[3]  
AVILA MA, 1994, CANCER RES, V54, P2424
[4]   Cyclooxygenase inhibitors induce the expression of the tumor suppressor gene EGR-1, which results in the up-regulation of NAG-1, an antitumorigenic protein [J].
Baek, SJ ;
Kim, JS ;
Moore, SM ;
Lee, SH ;
Martinez, J ;
Eling, TE .
MOLECULAR PHARMACOLOGY, 2005, 67 (02) :356-364
[5]   Epicatechin gallate-induced expression of NAG-1 is associated with growth inhibition and apoptosis in colon cancer cells [J].
Baek, SJ ;
Kim, JS ;
Jackson, FR ;
Eling, TE ;
McEntee, MF ;
Lee, SH .
CARCINOGENESIS, 2004, 25 (12) :2425-2432
[6]   Expression of NAG-1, a transforming growth factor-β superfamily member, by troglitazone requires the early growth response gene EGR-1 [J].
Baek, SJ ;
Kim, JS ;
Nixon, JB ;
DiAugustine, RP ;
Eling, TE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (08) :6883-6892
[7]   Dual function of nonsteroidal anti-inflammatory drugs (NSAIDs): Inhibition of cyclooxygenase and induction of NSAID-activated gene [J].
Baek, SJ ;
Wilson, LC ;
Lee, CH ;
Eling, TE .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 301 (03) :1126-1131
[8]   Resveratrol enhances the expression of non-steroidal anti-inflammatory drug-activated gene (NAG-1) by increasing the expression of p53 [J].
Baek, SJ ;
Wilson, LC ;
Eling, TE .
CARCINOGENESIS, 2002, 23 (03) :425-434
[9]   Cyclooxygenase inhibitors regulate the expression of a TGF-β superfamily member that has proapoptotic and antitumorigenic activities [J].
Baek, SJ ;
Kim, KS ;
Nixon, JB ;
Wilson, LC ;
Eling, TE .
MOLECULAR PHARMACOLOGY, 2001, 59 (04) :901-908
[10]   MIC-1, a novel macrophage inhibitory cytokine, is a divergent member of the TGF-beta superfamily [J].
Bootcov, MR ;
Bauskin, AR ;
Valenzuela, SM ;
Moore, AG ;
Bansal, M ;
He, XY ;
Zhang, HP ;
Donnellan, M ;
Mahler, S ;
Pryor, K ;
Walsh, BJ ;
Nicholson, RC ;
Fairlie, WD ;
Por, SB ;
Robbins, JM ;
Breit, SN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11514-11519